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1,4-Hexadiene, 2-methyl-, (E)-, also known as (E)-2-Methyl-1,4-hexadiene, is an organic compound with the molecular formula C7H12. It is a colorless liquid with a strong, pungent odor. This chemical is a conjugated diene, which means it has two carbon-carbon double bonds separated by a single bond, and it is a member of the alkene class of hydrocarbons. The (E)- configuration indicates that the two methyl groups are on the same side of the double bond. 1,4-Hexadiene, 2-methyl-, (E)- is used as a chemical intermediate in the synthesis of various organic compounds and can be found in the fragrance and flavoring industry. It is also used in the production of polymers and as a solvent. Due to its reactive nature, it is important to handle 1,4-Hexadiene, 2-methyl-, (E)- with care, as it can be flammable and may cause irritation to the skin, eyes, and respiratory system.

6108-96-9

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6108-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6108-96-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,0 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6108-96:
(6*6)+(5*1)+(4*0)+(3*8)+(2*9)+(1*6)=89
89 % 10 = 9
So 6108-96-9 is a valid CAS Registry Number.

6108-96-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-2-methyl-1,4-hexadiene

1.2 Other means of identification

Product number -
Other names 2-methyl-1,4-hexadiene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6108-96-9 SDS

6108-96-9Downstream Products

6108-96-9Relevant academic research and scientific papers

THE REDUCTION OF 2-VINYL-1,1-BIS(BROMOMETHYL)CYCLOPROPANE

Zefirov, N. S.,Kozhushkov, S. I.,Kuznetsova, T. S.,Sosonkin, I. M.,Domarev,A. M.,et al

, p. 1863 - 1873 (2007/10/02)

A study was carried out on the reduction of 2-vinyl-1,1-bis(bromomethyl)cyclopropane by various methods including electrochemical procedures.The major reaction pathways ential opening and expansion of the cyclopropane ring, while the product of the formation of a second three-membered ring, namely, vinylspiropentane, is formed in low yield.The probable radical mechanism for this reaction is discussed.

MECHANISM OF THE REACTION OF GLYCIDYL ESTERS WITH CARBOXYLIC ACIDS

Klebanov, M. S.,Kir'yazev, F. Yu.,Chervinskii, A. Yu.,Shologon, I. M.

, p. 2193 - 2196 (2007/10/02)

The kinetics of the reactions of 1-phenoxy-2,3-epoxypropane and 2,3-epoxypropylbenzoate with carboxylic acids were investigated.A new reaction mechanism is proposed to explain the anomalously high reactivity of the glycidyl esters.The mechanism involves protonation of the oxygen of the carbonyl group in the ester followed by intramolecular electrophilic attack on the oxirane oxygen by the carbonyl carbon atom, accompanied by opening of the epoxide ring and transfer of the acyl fragment in the glycidyl ester molecule.

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